6avh: Difference between revisions
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==GH3.15 acyl acid amido synthetase== | ==GH3.15 acyl acid amido synthetase== | ||
<StructureSection load='6avh' size='340' side='right' caption='[[6avh]], [[Resolution|resolution]] 3.01Å' scene=''> | <StructureSection load='6avh' size='340' side='right'caption='[[6avh]], [[Resolution|resolution]] 3.01Å' scene=''> | ||
== Structural highlights == | == Structural highlights == | ||
<table><tr><td colspan='2'>[[6avh]] is a 4 chain structure with sequence from [ | <table><tr><td colspan='2'>[[6avh]] is a 4 chain structure with sequence from [https://en.wikipedia.org/wiki/Arabidopsis_thaliana Arabidopsis thaliana]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=6AVH OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=6AVH FirstGlance]. <br> | ||
</td></tr><tr id=' | </td></tr><tr id='method'><td class="sblockLbl"><b>[[Empirical_models|Method:]]</b></td><td class="sblockDat" id="methodDat">X-ray diffraction, [[Resolution|Resolution]] 3.011Å</td></tr> | ||
<tr id=' | <tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat" id="ligandDat"><scene name='pdbligand=AMP:ADENOSINE+MONOPHOSPHATE'>AMP</scene></td></tr> | ||
<tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[ | <tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[https://proteopedia.org/fgij/fg.htm?mol=6avh FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=6avh OCA], [https://pdbe.org/6avh PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=6avh RCSB], [https://www.ebi.ac.uk/pdbsum/6avh PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=6avh ProSAT]</span></td></tr> | ||
</table> | </table> | ||
== Function == | |||
[https://www.uniprot.org/uniprot/GH315_ARATH GH315_ARATH] Indole-3-acetic acid-amido (IAA) synthetase that catalyzes the conjugation of amino acids to auxin specifically using the auxin precursor indole-3-butyric acid (IBA) and glutamine and, possibly, cysteine as substrates (PubMed:29462792, PubMed:30315112). Displays high catalytic activity with the auxinic phenoxyalkanoic acid herbicides 4-(2,4-dichlorophenoxy)butyric acid (2,4-DB) and to some extent 2,4-dichlorophenoxylacetic acid (2,4-D) as substrates, thus conferring resistance to herbicides (PubMed:30315112).<ref>PMID:29462792</ref> <ref>PMID:30315112</ref> | |||
<div style="background-color:#fffaf0;"> | <div style="background-color:#fffaf0;"> | ||
== Publication Abstract from PubMed == | == Publication Abstract from PubMed == | ||
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__TOC__ | __TOC__ | ||
</StructureSection> | </StructureSection> | ||
[[Category: | [[Category: Arabidopsis thaliana]] | ||
[[Category: | [[Category: Large Structures]] | ||
[[Category: | [[Category: Jez JM]] | ||
[[Category: | [[Category: Sherp AM]] | ||
Latest revision as of 09:42, 23 October 2024
GH3.15 acyl acid amido synthetase
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